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Items: 1 to 20 of 31

1.
A Homozygous Loss-of-Function Mutation in MSH5 Abolishes MutSγ Axial Loading and Causes Meiotic Arrest in NOA-Affected Individuals
Chenjia Gong, Tanveer Abbas, Zubair Muhammad, Jianteng Zhou, Ranjha Khan, Hui Ma, Huan Zhang, Qinghua Shi, Baolu Shi
Int J Mol Sci. 2022 Jun; 23(12): 6522. Published online 2022 Jun 10. doi: 10.3390/ijms23126522
PMCID:
PMC9224491
AbstractArticlePDF–7.7M
2.
MutS Homologue hMSH5: Recombinational DSB Repair and Non-Synonymous Polymorphic Variants
Xiling Wu, Yang Xu, Katey Feng, Joshua D. Tompkins, Chengtao Her
PLoS One. 2013; 8(9): e73284. Published online 2013 Sep 4. doi: 10.1371/journal.pone.0073284
PMCID:
PMC3762724
AbstractArticlePDF–1.4M
3.
hMSH5 is a nucleocytoplasmic shuttling protein whose stability depends on its subcellular localization
François Lahaye, Françoise Lespinasse, Pascal Staccini, Lucile Palin, Véronique Paquis-Flucklinger, Sabine Santucci-Darmanin
Nucleic Acids Res. 2010 Jun; 38(11): 3655–3671. Published online 2010 Feb 25. doi: 10.1093/nar/gkq098
PMCID:
PMC2887964
AbstractArticlePDF–5.1M
4.
Mutations of MSH5 in nonobstructive azoospermia (NOA) and rescued via in vivo gene editing
Min Chen, Chencheng Yao, Yingying Qin, Xiuhong Cui, Peng Li, Zhiyong Ji, Limei Lin, Haowei Wu, Zhi Zhou, Yaoting Gui, Zheng Li, Fei Gao
Signal Transduct Target Ther. 2022; 7: 1. Published online 2022 Jan 3. doi: 10.1038/s41392-021-00710-4
PMCID:
PMC8724278
ArticlePDF–1.6M
5.
Mutations in MSH5 in primary ovarian insufficiency
Ting Guo, Shidou Zhao, Shigang Zhao, Min Chen, Guangyu Li, Xue Jiao, Zhao Wang, Yueran Zhao, Yingying Qin, Fei Gao, Zi-Jiang Chen
Hum Mol Genet. 2017 Apr 15; 26(8): 1452–1457. Published online 2017 Feb 8. doi: 10.1093/hmg/ddx044
PMCID:
PMC5393145
AbstractArticlePDF–615K
6.
hMSH5 Facilitates the Repair of Camptothecin-induced Double-strand Breaks through an Interaction with FANCJ
Yang Xu, Xiling Wu, Chengtao Her
J Biol Chem. 2015 Jul 24; 290(30): 18545–18558. Published online 2015 Jun 8. doi: 10.1074/jbc.M115.642884
PMCID:
PMC4513114
AbstractArticlePDF–3.4M
7.
hMSH4-hMSH5 Adenosine Nucleotide Processing and Interactions with Homologous Recombination Machinery
Timothy Snowden, Kang-Sup Shim, Christoph Schmutte, Samir Acharya, Richard Fishel
J Biol Chem. Author manuscript; available in PMC 2010 Mar 18.
Published in final edited form as: J Biol Chem. 2008 Jan 4; 283(1): 145–154. Published online 2007 Oct 30. doi: 10.1074/jbc.M704060200
PMCID:
PMC2841433
AbstractArticlePDF–1.5M
8.
Long noncoding RNA HCP5 participates in premature ovarian insufficiency by transcriptionally regulating MSH5 and DNA damage repair via YB1
Xiaoyan Wang, Xinyue Zhang, Yujie Dang, Duan Li, Gang Lu, Wai-Yee Chan, Peter C K Leung, Shidou Zhao, Yingying Qin, Zi-Jiang Chen
Nucleic Acids Res. 2020 May 7; 48(8): 4480–4491. Published online 2020 Feb 29. doi: 10.1093/nar/gkaa127
PMCID:
PMC7192606
AbstractArticlePDF–3.3M
9.
MutS homologue hMSH5: role in cisplatin-induced DNA damage response
Joshua D Tompkins, Xiling Wu, Chengtao Her
Mol Cancer. 2012; 11: 10. Published online 2012 Mar 8. doi: 10.1186/1476-4598-11-10
PMCID:
PMC3325843
AbstractArticlePDF–3.3M
10.
Evidence for a direct involvement of hMSH5 in promoting ionizing radiation induced apoptosis
JOSHUA D. TOMPKINS, XILING WU, YEN-LIN CHU, CHENGTAO HER
Exp Cell Res. Author manuscript; available in PMC 2011 Sep 13.
Published in final edited form as: Exp Cell Res. 2009 Aug 15; 315(14): 2420–2432. Published online 2009 May 12. doi: 10.1016/j.yexcr.2009.05.004
PMCID:
PMC3171649
AbstractArticlePDF–1.9M
11.
PCNA activates the MutLγ endonuclease to promote meiotic crossing over
Dhananjaya S. Kulkarni, Shannon N. Owens, Masayoshi Honda, Masaru Ito, Ye Yang, Mary W. Corrigan, Lan Chen, Aric L. Quan, Neil Hunter
Nature. Author manuscript; available in PMC 2021 Jul 16.
Published in final edited form as: Nature. 2020 Oct; 586(7830): 623–627. Published online 2020 Aug 19. doi: 10.1038/s41586-020-2645-6
Correction in:
Nature. 2021 Jan 19
PMCID:
PMC8284803
AbstractArticlePDF–4.8M
12.
Common 5p15.33 and 6p21.33 variants influence lung cancer risk
Yufei Wang, Peter Broderick, Emily Webb, Xifeng Wu, Jayaram Vijayakrishnan, Athena Matakidou, Mobshra Qureshi, Qiong Dong, Xiangjun Gu, Wei Vivien Chen, Margaret R Spitz, Timothy Eisen, Christopher I Amos, Richard S Houlston
Nat Genet. Author manuscript; available in PMC 2009 Dec 1.
Published in final edited form as: Nat Genet. 2008 Dec; 40(12): 1407–1409. Published online 2008 Nov 2. doi: 10.1038/ng.273
PMCID:
PMC2695928
AbstractArticlePDF–798K
13.
Role for Msh5 in the regulation of Ig class switch recombination
Hideharu Sekine, Ricardo C. Ferreira, Qiang Pan-Hammarström, Robert R. Graham, Beth Ziemba, Sandra S. de Vries, Jiabin Liu, Keli Hippen, Thearith Koeuth, Ward Ortmann, Akiko Iwahori, Margaret K. Elliott, Steven Offer, Cara Skon, Likun Du, Jill Novitzke, Annette T. Lee, Nianxi Zhao, Joshua D. Tompkins, David Altshuler, Peter K. Gregersen, Charlotte Cunningham-Rundles, Reuben S. Harris, Chengtao Her, David L. Nelson, Lennart Hammarström, Gary S. Gilkeson, Timothy W. Behrens
Proc Natl Acad Sci U S A. 2007 Apr 24; 104(17): 7193–7198. Published online 2007 Apr 4. doi: 10.1073/pnas.0700815104
PMCID:
PMC1855370
AbstractArticlePDF–865K
14.
Identification of multiple HTF-island associated genes in the human major histocompatibility complex class III region.
C A Sargent, I Dunham, R D Campbell
EMBO J. 1989 Aug; 8(8): 2305–2312. doi: 10.1002/j.1460-2075.1989.tb08357.x
PMCID:
PMC401163
SummaryPage BrowsePDF–1.9M
15.
Association between DNA mismatch repair gene polymorphisms and platinum-based chemotherapy toxicity in non-small cell lung cancer patients
Jun-Yan Liu, Chen-Yue Qian, Yuan-Feng Gao, Juan Chen, Hong-Hao Zhou, Ji-Ye Yin
Chin J Cancer. 2017; 36: 12. Published online 2017 Jan 16. doi: 10.1186/s40880-016-0175-2
PMCID:
PMC5238520
AbstractArticlePDF–1.0M
16.
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
The International Consortium for Systemic Lupus Erythematosus Genetics (SLEGEN), John B Harley, Marta E Alarcón-Riquelme, Lindsey A Criswell, Chaim O Jacob, Robert P Kimberly, Kathy L Moser, Betty P Tsao, Timothy J Vyse, Carl D Langefeld, Swapan K Nath, Joel M Guthridge, Beth L Cobb, Daniel B Mirel, Miranda C Marion, Adrienne H Williams, Jasmin Divers, Wei Wang, Summer G Frank, Bahram Namjou, Stacey B Gabriel, Annette T Lee, Peter K Gregersen, Timothy W Behrens, Kimberly E Taylor, Michelle Fernando, Raphael Zidovetzki, Patrick M Gaffney, Jeffrey C Edberg, John D Rioux, Joshua O Ojwang, Judith A James, Joan T Merrill, Gary S Gilkeson, Michael F Seldin, Hong Yin, Emily C Baechler, Quan-Zhen Li, Edward K Wakeland, Gail R Bruner, Kenneth M Kaufman, Jennifer A Kelly
Nat Genet. Author manuscript; available in PMC 2013 Jul 16.
Published in final edited form as: Nat Genet. 2008 Feb; 40(2): 204–210. Published online 2008 Jan 20. doi: 10.1038/ng.81
PMCID:
PMC3712260
AbstractArticlePDF–458K
17.
Genetically Determined Amerindian Ancestry Correlates with Increased Frequency of Risk Alleles for Systemic Lupus Erythematosus
E Sanchez, R Webb, A. Rasmussen, J.A Kelly, L. Riba, K.M. Kaufman, I. Garcia-de la Torre, J.F. Moctezuma, M.A. Maradiaga-Ceceña, M. Cardiel, E. Acevedo, M. Cucho-Venegas, M.A. Garcia, S. Gamron, B.A. Pons-Estel, C. Vasconcelos, J. Martin, T. Tusié-Luna, J.B. Harley, B. Richardson, A.H. Sawalha, M.E. Alarcón-Riquelme
Arthritis Rheum. Author manuscript; available in PMC 2011 Dec 1.
Published in final edited form as: Arthritis Rheum. 2010 Dec; 62(12): 3722–3729. doi: 10.1002/art.27753
PMCID:
PMC3078084
AbstractArticlePDF–200K
18.
Association of MHC SNP genotype with susceptibility to type 1 diabetes: a modified survival approach
E. McKinnon, G. Morahan, D. Nolan, I. James, the Type 1 Diabetes Genetics Consortium
Diabetes Obes Metab. Author manuscript; available in PMC 2009 Oct 2.
Published in final edited form as: Diabetes Obes Metab. 2009 Feb; 11(Suppl 1): 92–100. doi: 10.1111/j.1463-1326.2008.01009.x
PMCID:
PMC2755510
AbstractArticlePDF–1.1M
19.
Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1
A. M. Valdes, G. Thomson, Type 1 Diabetes Genetics Consortium
Diabetes Obes Metab. Author manuscript; available in PMC 2009 Oct 1.
Published in final edited form as: Diabetes Obes Metab. 2009 Feb; 11(Suppl 1): 46–52. doi: 10.1111/j.1463-1326.2008.01002.x
PMCID:
PMC2755069
AbstractArticlePDF–548K
20.
HSP90 shapes the consequences of human genetic variation
Georgios I. Karras, Song Yi, Nidhi Sahni, Máté Fischer, Jenny Xie, Marc Vidal, Alan D. D'Andrea, Luke Whitesell, Susan Lindquist
Cell. Author manuscript; available in PMC 2018 Feb 23.
Published in final edited form as: Cell. 2017 Feb 23; 168(5): 856–866.e12. Published online 2017 Feb 16. doi: 10.1016/j.cell.2017.01.023
PMCID:
PMC5325763
AbstractArticlePDF–2.4M

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